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Multi-quantum quadrupole relaxation enhancement effects in 209Bi compounds.
Kruk, D; Umut, E; Masiewicz, E; Fischer, R; Scharfetter, H.
Afiliação
  • Kruk D; Faculty of Mathematics and Computer Science, University of Warmia and Mazury in Olsztyn, Sloneczna 54, PL-10710 Olsztyn, Poland.
  • Umut E; Faculty of Mathematics and Computer Science, University of Warmia and Mazury in Olsztyn, Sloneczna 54, PL-10710 Olsztyn, Poland.
  • Masiewicz E; Faculty of Mathematics and Computer Science, University of Warmia and Mazury in Olsztyn, Sloneczna 54, PL-10710 Olsztyn, Poland.
  • Fischer R; Institute of Inorganic Chemistry, Graz University of Technology, Stremayrgasse 9/V, A-8010 Graz, Austria.
  • Scharfetter H; Institute of Medical Engineering, Graz University of Technology, Stremayrgasse 16/III, A-8010 Graz, Austria.
J Chem Phys ; 150(18): 184309, 2019 May 14.
Article em En | MEDLINE | ID: mdl-31091937
ABSTRACT
1H spin-lattice nuclear magnetic resonance relaxation experiments have been performed for triphenylbismuth dichloride (C18H15BiCl2) and phenylbismuth dichloride (C6H5BiCl2) in powder. The frequency range of 20-128 MHz has been covered. Due to 1H-209Bi dipole-dipole interactions, a rich set of pronounced Quadrupole Relaxation Enhancement (QRE) peaks (quadrupole peaks) has been observed. The QRE patterns for both compounds have been explained in terms of single- and double-quantum transitions of the participating nuclei. The analysis has revealed a complex, quantum-mechanical mechanism of the QRE effects. The mechanism goes far beyond the simple explanation of the existence of three quadrupole peaks for 14N reported in literature. The analysis has been supported by nuclear quadrupole resonance results that independently provided the 209Bi quadrupole parameters (amplitude of the quadrupole coupling constant and asymmetry parameter).

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Chem Phys Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Polônia

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Chem Phys Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Polônia